Variant #0000973720 (NC_000001.10:g.226054304_226054305del, NM_014698.2:c.645_646del (TMEM63A))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.226054304_226054305del
DNA change (hg38) -
Published as TMEM63A(NM_014698.3):c.645_646del (p.(Gln216ValfsTer3))
ISCN -
DB-ID EPHX1_000026
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPHX1 NM_000120.3 ?/. - c.*21256_*21257del r.(=) p.(=)
TMEM63A NM_014698.2 ?/. - c.645_646del r.(?) p.(Gln216Valfs*3)


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